Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
rs12153855 | 0.776 | 0.320 | 6 | 32107027 | intron variant | T/C | snv | 0.11 | 10 | ||
rs2516049 | 0.742 | 0.400 | 6 | 32602623 | intergenic variant | T/C | snv | 0.27 | 9 | ||
rs12198173 | 0.827 | 0.240 | 6 | 32059031 | intron variant | G/A | snv | 0.10 | 9 | ||
rs2395185 | 0.724 | 0.360 | 6 | 32465390 | intron variant | G/T | snv | 0.29 | 8 | ||
rs10484554 | 0.807 | 0.200 | 6 | 31306778 | intron variant | C/T | snv | 0.12 | 8 | ||
rs13199524 | 0.807 | 0.240 | 6 | 32098988 | intron variant | C/T | snv | 8.4E-02 | 8 | ||
rs1464510 | 0.807 | 0.280 | 3 | 188394766 | intron variant | C/A;T | snv | 7 | |||
rs3130473 | 0.882 | 0.160 | 6 | 31231431 | intergenic variant | C/T | snv | 0.23 | 6 | ||
rs3132580 | 0.790 | 0.360 | 6 | 30952347 | missense variant | G/A | snv | 8.0E-02 | 9.3E-02 | 6 | |
rs3131296 | 0.807 | 0.320 | 6 | 32205216 | intron variant | C/T | snv | 0.11 | 6 | ||
rs3134942 | 0.790 | 0.320 | 6 | 32200994 | synonymous variant | G/T | snv | 9.7E-02 | 0.11 | 6 | |
rs13211318 | 0.925 | 0.040 | 6 | 32134903 | upstream gene variant | A/C | snv | 0.11 | 5 | ||
rs3130424 | 0.925 | 0.040 | 6 | 31250462 | intergenic variant | A/C;G;T | snv | 5 | |||
rs4766578 | 0.851 | 0.200 | 12 | 111466567 | intron variant | T/A | snv | 0.66 | 5 | ||
rs3806156 | 0.827 | 0.280 | 6 | 32405921 | intron variant | G/A;T | snv | 5 | |||
rs2524123 | 0.925 | 0.040 | 6 | 31297537 | intron variant | T/C | snv | 0.34 | 5 | ||
rs12203592 | 0.649 | 0.320 | 6 | 396321 | intron variant | C/T | snv | 0.10 | 5 | ||
rs1701704 | 0.851 | 0.200 | 12 | 56018703 | intron variant | T/G | snv | 0.25 | 5 | ||
rs34214527 | 0.925 | 0.040 | 6 | 32046679 | intron variant | C/T | snv | 0.11 | 5 | ||
rs11203203 | 0.807 | 0.240 | 21 | 42416077 | intron variant | G/A | snv | 0.28 | 5 | ||
rs769449 | 0.882 | 0.120 | 19 | 44906745 | non coding transcript exon variant | G/A | snv | 8.4E-02 | 4 | ||
rs1393350 | 0.851 | 0.160 | 11 | 89277878 | intron variant | G/A | snv | 0.17 | 4 | ||
rs4409785 | 0.752 | 0.240 | 11 | 95578258 | intron variant | T/C | snv | 0.13 | 3 | ||
rs968567 | 0.851 | 0.240 | 11 | 61828092 | intron variant | C/T | snv | 0.11 | 3 |